Variant report

Variant	nsv3598
Chromosome Location	chr1:173693027-173738687
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr1:173729420-173729866	K562	blood:	n/a	n/a
2	CEBPB	chr1:173727312-173727508	K562	blood:	n/a	n/a
3	CEBPB	chr1:173701289-173701317	K562	blood:	n/a	n/a
4	CEBPB	chr1:173719695-173719770	HepG2	liver:	n/a	n/a
5	CEBPB	chr1:173719651-173719764	IMR90	lung:	n/a	chr1:173719680-173719691
6	CEBPB	chr1:173719658-173719748	K562	blood:	n/a	chr1:173719680-173719691
7	CEBPB	chr1:173719656-173719776	H1-hESC	embryonic stem cell:	n/a	chr1:173719680-173719691
8	CEBPB	chr1:173727276-173727484	A549	lung:	n/a	n/a
9	CTCF	chr1:173714357-173714399	MCF-7	breast:	n/a	n/a
10	CTCF	chr1:173705415-173705528	GM20000	blood:	n/a	n/a
11	CTCF	chr1:173727434-173727488	GM20000	blood:	n/a	n/a
12	CTCF	chr1:173727920-173728070	HBMEC	blood vessel:	n/a	n/a
13	E2F6	chr1:173728127-173728338	K562	blood:	n/a	n/a
14	FOS	chr1:173728300-173728313	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr1:173728242-173728344	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr1:173737492-173737568	MCF10A-Er-Src	breast:	n/a	chr1:173737520-173737530 chr1:173737521-173737529 chr1:173737522-173737529
17	FOXA1	chr1:173723034-173723312	HepG2	liver:	n/a	n/a
18	FOXA1	chr1:173695141-173695458	HepG2	liver:	n/a	n/a
19	GATA3	chr1:173737081-173737107	SH-SY5Y	brain:	n/a	n/a
20	GATA3	chr1:173701909-173702063	SH-SY5Y	brain:	n/a	n/a
21	GATA3	chr1:173713009-173713065	SH-SY5Y	brain:	n/a	n/a
22	GATA3	chr1:173712593-173712637	SH-SY5Y	brain:	n/a	n/a
23	HCFC1	chr1:173703355-173703376	K562	blood:	n/a	n/a
24	HNF4A	chr1:173723024-173723279	HepG2	liver:	n/a	chr1:173723184-173723199 chr1:173723186-173723198 chr1:173723184-173723199 chr1:173723185-173723199 chr1:173723185-173723197 chr1:173723186-173723198 chr1:173723186-173723199 chr1:173723184-173723199 chr1:173723186-173723198 chr1:173723185-173723198 chr1:173723181-173723203 chr1:173723184-173723199 chr1:173723185-173723199 chr1:173723183-173723201 chr1:173723185-173723199 chr1:173723185-173723200 chr1:173723186-173723199 chr1:173723186-173723199
25	IRF1	chr1:173717019-173717088	K562	blood:	n/a	n/a
26	IRF1	chr1:173723042-173723195	K562	blood:	n/a	chr1:173723141-173723151 chr1:173723140-173723157 chr1:173723147-173723157 chr1:173723139-173723159 chr1:173723140-173723152 chr1:173723141-173723152 chr1:173723148-173723164 chr1:173723143-173723157 chr1:173723141-173723155 chr1:173723147-173723161 chr1:173723137-173723151
27	IRF1	chr1:173716292-173716310	K562	blood:	n/a	n/a
28	IRF3	chr1:173694444-173694540	GM12878	blood:	n/a	n/a
29	JUN	chr1:173725079-173725142	H1-hESC	embryonic stem cell:	n/a	n/a
30	JUN	chr1:173703803-173703818	K562	blood:	n/a	n/a
31	JUND	chr1:173727406-173727520	HepG2	liver:	n/a	n/a
32	MAFF	chr1:173720384-173720530	K562	blood:	n/a	n/a
33	MAFF	chr1:173721028-173721258	HepG2	liver:	n/a	chr1:173721084-173721102
34	MAFK	chr1:173711141-173711234	HepG2	liver:	n/a	n/a
35	MAFK	chr1:173720913-173721250	IMR90	lung:	n/a	chr1:173721086-173721101
36	MAFK	chr1:173720982-173721273	HepG2	liver:	n/a	chr1:173721086-173721101
37	MAFK	chr1:173720982-173721232	HepG2	liver:	n/a	chr1:173721086-173721101
38	MAFK	chr1:173719177-173719291	HepG2	liver:	n/a	n/a
39	MAFK	chr1:173720408-173720513	Hela-S3	cervix:	n/a	chr1:173720478-173720489 chr1:173720477-173720491 chr1:173720478-173720489 chr1:173720479-173720490
40	MAFK	chr1:173720413-173720617	HepG2	liver:	n/a	chr1:173720478-173720489 chr1:173720477-173720491 chr1:173720538-173720554 chr1:173720536-173720556 chr1:173720539-173720553 chr1:173720478-173720489 chr1:173720479-173720490
41	MYC	chr1:173719483-173719601	MCF-7	breast:	n/a	n/a
42	NRF1	chr1:173718108-173718227	GM12878	blood:	n/a	n/a
43	POLR2A	chr1:173735346-173735350	Gliobla	brain:	n/a	n/a
44	POLR2A	chr1:173719485-173719606	MCF-7	breast:	n/a	n/a
45	POLR2A	chr1:173722176-173722266	K562	blood:	n/a	n/a
46	POLR2A	chr1:173710747-173710917	GM12878	blood:	n/a	n/a
47	POLR2A	chr1:173708293-173708344	HepG2	liver:	n/a	n/a
48	POLR2A	chr1:173719492-173719560	MCF-7	breast:	n/a	n/a
49	POLR2A	chr1:173707438-173707505	HepG2	liver:	n/a	n/a
50	POLR2A	chr1:173712827-173712843	ProgFib	skin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:173713824..173715572-chr1:173738278..173740994,2	K562	blood:
2	chr1:173702803..173705029-chr1:173705548..173707166,2	K562	blood:
3	chr1:173684004..173686293-chr1:173689052..173693084,4	MCF-7	breast:
4	chr1:173737933..173739972-chr1:173748335..173750553,2	MCF-7	breast:
5	chr1:173713824..173715572-chr1:173738278..173740994,2	K562	blood:
6	chr1:173708791..173710974-chr1:173715096..173717905,2	MCF-7	breast:
7	chr1:173733973..173736471-chr1:173739138..173740675,2	K562	blood:
8	chr1:173727893..173730876-chr1:173792741..173795143,2	K562	blood:
9	chr1:173684039..173685629-chr1:173712424..173714530,2	MCF-7	breast:
10	chr1:173691682..173694241-chr1:173700147..173703100,2	K562	blood:
11	chr1:173735243..173738226-chr1:173747475..173749570,2	K562	blood:
12	chr1:173718954..173722251-chr1:173724534..173727033,3	MCF-7	breast:
13	chr1:173687895..173689585-chr1:173692482..173695234,2	MCF-7	breast:
14	chr1:173684000..173686822-chr1:173693037..173695144,2	K562	blood:
15	chr1:173445732..173447844-chr1:173719018..173720603,2	MCF-7	breast:
16	chr1:173701895..173703429-chr1:173835621..173837927,2	MCF-7	breast:
17	chr1:173683476..173686159-chr1:173702055..173703669,2	K562	blood:
18	chr1:173718954..173722251-chr1:173724534..173727033,3	MCF-7	breast:
19	chr1:173693597..173695637-chr1:173710759..173712908,2	MCF-7	breast:
20	chr1:173702803..173705029-chr1:173705548..173707166,2	K562	blood:
21	chr1:173720884..173724693-chr1:173791444..173794240,3	K562	blood:
22	chr1:173710013..173713687-chr1:173714145..173716947,3	K562	blood:
23	chr1:173691682..173694241-chr1:173700147..173703100,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL20-2	chr1:173702852-173702967	NONHSAT007648
2	lnc-DARS2-4	chr1:173710813-173711067	NONHSAT007649

Variant related genes	Relation type
ENSG00000225591	TF binding region
ENSG00000225591	chromatin interactions
ENSG00000120334	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000117592	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000076321	chromatin interactions
ENSG00000117593	chromatin interactions

Extended variants
information (count: 1613 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563823193	chr1:173693030-173693031	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577329263	chr1:173693034-173693035	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs74475932	chr1:173693149-173693150	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs140366366	chr1:173693162-173693163	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528739870	chr1:173693188-173693189	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs149629808	chr1:173693213-173693214	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139462621	chr1:173693266-173693267	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562052941	chr1:173693269-173693270	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs548506074	chr1:173693275-173693276	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs375714592	chr1:173693311-173693312	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs571599460	chr1:173693312-173693313	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs560515125	chr1:173693339-173693340	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs145427819	chr1:173693369-173693370	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs527731870	chr1:173693381-173693382	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs549565430	chr1:173693390-173693391	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547550078	chr1:173693450-173693451	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs188036348	chr1:173693509-173693510	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs193096339	chr1:173693539-173693540	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs538394722	chr1:173693555-173693556	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs552344560	chr1:173693681-173693682	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs7513315	chr1:173693694-173693695	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs185862906	chr1:173693745-173693746	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs188888901	chr1:173693762-173693763	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs71643168	chr1:173693766-173693767	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs114198073	chr1:173693797-173693798	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs537443474	chr1:173693892-173693893	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs557120547	chr1:173693893-173693894	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs146463664	chr1:173693903-173693904	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs149062620	chr1:173693904-173693905	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs570956708	chr1:173693908-173693909	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs78873745	chr1:173693909-173693910	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs573118925	chr1:173693942-173693943	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs542090364	chr1:173693972-173693973	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs562047510	chr1:173693976-173693977	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs116185683	chr1:173694066-173694067	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs549740365	chr1:173694142-173694143	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs563184071	chr1:173694150-173694151	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs543333869	chr1:173694218-173694219	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs6658217	chr1:173694231-173694232	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs61826814	chr1:173694259-173694260	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs549918177	chr1:173694271-173694272	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs569520598	chr1:173694285-173694286	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs114021790	chr1:173694331-173694332	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs528315171	chr1:173694356-173694357	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs373894835	chr1:173694360-173694361	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs539589034	chr1:173694371-173694372	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs61826815	chr1:173694408-173694409	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs372815160	chr1:173694425-173694426	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs536996008	chr1:173694456-173694457	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs202121771	chr1:173694478-173694479	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD
Autism	22495309	CNVD

Chromatin state (count:1242 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173684800-173695000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:173684800-173702800	Weak transcription	Spleen	Spleen
3	chr1:173685000-173695200	Weak transcription	Esophagus	oesophagus
4	chr1:173685000-173695200	Weak transcription	Pancreas	Pancrea
5	chr1:173685000-173720800	Weak transcription	Small Intestine	intestine
6	chr1:173685200-173693400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:173685200-173694000	Weak transcription	Left Ventricle	heart
8	chr1:173685200-173694200	Weak transcription	Brain Hippocampus Middle	brain
9	chr1:173685200-173694400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:173685200-173694400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr1:173685200-173694400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:173685200-173694400	Weak transcription	Brain Cingulate Gyrus	brain
13	chr1:173685200-173694400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr1:173685200-173694600	Weak transcription	Colonic Mucosa	Colon
15	chr1:173685200-173724600	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr1:173685400-173694000	Weak transcription	Primary B cells from peripheral blood	blood
17	chr1:173685400-173694200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr1:173685400-173694400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr1:173685400-173694400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr1:173685400-173694400	Weak transcription	Fetal Brain Male	brain
21	chr1:173685400-173702800	Weak transcription	Psoas Muscle	Psoas
22	chr1:173685400-173725000	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr1:173685600-173693800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr1:173685600-173694200	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr1:173685600-173694600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr1:173685600-173702800	Weak transcription	Brain Substantia Nigra	brain
27	chr1:173685800-173693600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:173685800-173702800	Weak transcription	NH-A	brain
29	chr1:173685800-173703000	Weak transcription	Osteobl	bone
30	chr1:173685800-173724800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr1:173686000-173693800	Weak transcription	HMEC	breast
32	chr1:173686200-173694400	Weak transcription	NHLF	lung
33	chr1:173686200-173702800	Weak transcription	NHEK	skin
34	chr1:173686400-173694200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr1:173686600-173702800	Weak transcription	HSMMtube	muscle
36	chr1:173686800-173693800	Weak transcription	Adipose Nuclei	Adipose
37	chr1:173686800-173694200	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr1:173686800-173694200	Weak transcription	NHDF-Ad	bronchial
39	chr1:173686800-173694400	Weak transcription	Duodenum Mucosa	Duodenum
40	chr1:173686800-173694400	Weak transcription	Fetal Heart	heart
41	chr1:173686800-173694400	Weak transcription	Rectal Smooth Muscle	rectum
42	chr1:173686800-173694400	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr1:173686800-173702800	Weak transcription	Gastric	stomach
44	chr1:173686800-173703000	Weak transcription	Brain Angular Gyrus	brain
45	chr1:173686800-173721600	Weak transcription	HUVEC	blood vessel
46	chr1:173686800-173721800	Weak transcription	Colon Smooth Muscle	Colon
47	chr1:173686800-173725400	Weak transcription	Right Ventricle	heart
48	chr1:173687000-173694200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr1:173687000-173702800	Weak transcription	HepG2	liver
50	chr1:173687400-173694400	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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