Variant report

Variant	esv3425400
Chromosome Location	chr2:96655850-96658398
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	ARID3A	chr2:96657356-96657461	HepG2	liver:	n/a	n/a
2	BATF	chr2:96657475-96657892	GM12878	blood:	n/a	n/a
3	BCL11A	chr2:96657495-96657685	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:96657716-96658282	GM12878	blood:	n/a	chr2:96658121-96658134 chr2:96658034-96658047
5	BHLHE40	chr2:96658011-96658260	HepG2	liver:	n/a	chr2:96658035-96658051
6	BHLHE40	chr2:96657453-96657904	HepG2	liver:	n/a	n/a
7	BRCA1	chr2:96657456-96657485	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr2:96657325-96658290	K562	blood:	n/a	n/a
9	CEBPD	chr2:96657560-96657977	K562	blood:	n/a	n/a
10	CHD1	chr2:96657191-96657571	IMR90	lung:	n/a	n/a
11	CHD2	chr2:96657404-96657454	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr2:96658382-96658459	GM19240	blood:	n/a	n/a
13	CTCF	chr2:96657943-96658257	GM10266	blood:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
14	CTCF	chr2:96657906-96658239	MCF-7	breast:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
15	CTCF	chr2:96658050-96658158	HepG2	liver:	n/a	chr2:96658100-96658113
16	CTCF	chr2:96658260-96658410	HCFaa	heart:	n/a	n/a
17	CTCF	chr2:96657858-96658263	A549	lung:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
18	CTCF	chr2:96658384-96658468	Lung_OC	lung:	n/a	n/a
19	CTCF	chr2:96657828-96659075	K562	blood:	n/a	chr2:96658689-96658697 chr2:96658684-96658702 chr2:96658753-96658769 chr2:96658686-96658707 chr2:96658752-96658770 chr2:96658754-96658775 chr2:96658205-96658218 chr2:96658100-96658113
20	CTCF	chr2:96657967-96658227	ProgFib	skin:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
21	CTCF	chr2:96657611-96657791	GM10248	blood:	n/a	n/a
22	CTCF	chr2:96658385-96658412	GM12892	blood:	n/a	n/a
23	CTCF	chr2:96658259-96658277	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr2:96657940-96658238	GM19240	blood:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
25	CTCF	chr2:96658360-96658510	GM06990	blood:	n/a	n/a
26	CTCF	chr2:96657915-96658226	Lung_OC	lung:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
27	CTCF	chr2:96657679-96657722	LNCaP	prostate:	n/a	n/a
28	CTCF	chr2:96657681-96657704	NHEK	skin:	n/a	n/a
29	CTCF	chr2:96658000-96658146	HUVEC	blood vessel:	n/a	chr2:96658100-96658113
30	CTCF	chr2:96658340-96658490	GM12875	blood:	n/a	n/a
31	CTCF	chr2:96657840-96657990	HMEC	breast:	n/a	n/a
32	CTCF	chr2:96657880-96658030	HAc	cerebellar:	n/a	n/a
33	CTCF	chr2:96658391-96658397	GM10266	blood:	n/a	n/a
34	CTCF	chr2:96657636-96657790	GM10266	blood:	n/a	n/a
35	CTCF	chr2:96658280-96658430	GM12865	blood:	n/a	n/a
36	CTCF	chr2:96657840-96657990	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr2:96657900-96658050	K562	blood:	n/a	n/a
38	CTCF	chr2:96658280-96658430	GM12864	blood:	n/a	n/a
39	CTCF	chr2:96658340-96658490	HepG2	liver:	n/a	n/a
40	CTCF	chr2:96657879-96658242	K562	blood:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
41	CTCF	chr2:96657994-96658205	GM20000	blood:	n/a	chr2:96658100-96658113
42	CTCF	chr2:96657629-96657703	Fibrobl	skin:	n/a	n/a
43	CTCF	chr2:96657906-96658236	GM12891	blood:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
44	CTCF	chr2:96658360-96658510	SAEC	small airway:	n/a	n/a
45	CTCF	chr2:96657975-96658222	H1-hESC	embryonic stem cell:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
46	CTCF	chr2:96657865-96658267	A549	lung:	n/a	chr2:96658205-96658218 chr2:96658100-96658113
47	CTCF	chr2:96657608-96657801	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr2:96657880-96658030	GM12869	blood:	n/a	n/a
49	CTCF	chr2:96658300-96658450	NHLF	lung:	n/a	n/a
50	CTCF	chr2:96657643-96657791	GM13977	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96658020-96658070	MCF-7	breast:	n/a
2	chr2:96658020-96658070	MCF-7	breast:	n/a
3	chr2:96657499-96657549	PANC-1	pancreas:	n/a
4	chr2:96658020-96658070	AG09319	gingival:	n/a
5	chr2:96658324-96658374	SK-N-MC	brain:	n/a
6	chr2:96658324-96658374	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:96657499-96657549	HRCEpiC	kidney:	n/a
8	chr2:96658324-96658374	GM06990	blood:	n/a
9	chr2:96658324-96658374	PANC-1	pancreas:	n/a
10	chr2:96657499-96657549	U87	brain:	n/a
11	chr2:96657499-96657549	PFSK-1	brain:	n/a
12	chr2:96658020-96658070	HRCEpiC	kidney:	n/a
13	chr2:96658020-96658070	ovcar-3	ovarian:	n/a
14	chr2:96658020-96658070	SAEC	small airway:	n/a
15	chr2:96657499-96657549	AoSMC	blood vessel:	n/a
16	chr2:96658020-96658070	SK-N-MC	brain:	n/a
17	chr2:96657403-96657453	HRCEpiC	kidney:	n/a
18	chr2:96658324-96658374	NT2-D1	testis:	n/a
19	chr2:96657403-96657453	IMR90	lung:	fetal
20	chr2:96658020-96658070	A549	lung:	n/a
21	chr2:96658324-96658374	IMR90	lung:	fetal
22	chr2:96658324-96658374	NHDF-neo	bronchial:	n/a
23	chr2:96658324-96658374	NB4	blood:	n/a
24	chr2:96658020-96658070	HCF	heart:	n/a
25	chr2:96658324-96658374	SK-N-SH_RA	brain:	n/a
26	chr2:96658020-96658070	CMK	blood:	n/a
27	chr2:96657499-96657549	Caco-2	colon:	n/a
28	chr2:96658020-96658070	GM12891	blood:	n/a
29	chr2:96658324-96658374	HAEpiC	amniotic membrane:	n/a
30	chr2:96657403-96657453	HRPEpiC	eye:	n/a
31	chr2:96658324-96658374	U87	brain:	n/a
32	chr2:96658324-96658374	SAEC	small airway:	n/a
33	chr2:96657403-96657453	AG09309	skin:	n/a
34	chr2:96657499-96657549	ECC-1	luminal epithelium:	n/a
35	chr2:96657403-96657453	AG04449	skin:	fetal
36	chr2:96658324-96658374	HCF	heart:	n/a
37	chr2:96658324-96658374	MCF-7	breast:	n/a
38	chr2:96658020-96658070	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:96658324-96658374	NH-A	brain:	n/a
40	chr2:96658324-96658374	Caco-2	colon:	n/a
41	chr2:96657403-96657453	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:96658020-96658070	SK-N-SH_RA	brain:	n/a
43	chr2:96657499-96657549	LNCaP	prostate:	n/a
44	chr2:96657403-96657453	T-47D	breast:	n/a
45	chr2:96657403-96657453	HCF	heart:	n/a
46	chr2:96658020-96658070	Jurkat	blood:	n/a
47	chr2:96658020-96658070	NHDF-neo	bronchial:	n/a
48	chr2:96657499-96657549	AG04449	skin:	fetal
49	chr2:96658324-96658374	Hela-S3	cervix:	n/a
50	chr2:96657499-96657549	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:96656872..96660081-chr2:96874473..96876452,3	MCF-7	breast:
2	chr2:96656483..96658831-chr2:96781728..96784486,2	K562	blood:
3	chr2:96658361..96659117-chr2:98208510..98209019,2	MCF-7	breast:
4	chr2:96658288..96659130-chr2:96839638..96840848,4	MCF-7	breast:

Variant related genes	Relation type
ANKRD36C	TF binding region
ANKRD36C	CpG island
ENSG00000222040	chromatin interactions
ENSG00000084090	chromatin interactions

Extended variants
information (count: 57 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:57 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573636573	chr2:96655990-96655991	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs181328438	chr2:96656074-96656075	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs534764206	chr2:96656081-96656082	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs527755946	chr2:96656085-96656086	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs547986503	chr2:96656137-96656138	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs367804205	chr2:96656232-96656233	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539773456	chr2:96656251-96656252	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376068069	chr2:96656299-96656300	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184285554	chr2:96656356-96656357	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568555325	chr2:96656421-96656422	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs537460500	chr2:96656507-96656508	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189186244	chr2:96656518-96656519	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs2260906	chr2:96656551-96656552	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574487828	chr2:96656576-96656577	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2260905	chr2:96656630-96656631	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs553959191	chr2:96656634-96656635	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182248191	chr2:96656639-96656640	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs546159585	chr2:96656650-96656651	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552686412	chr2:96656822-96656823	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562778766	chr2:96657106-96657107	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs2918820	chr2:96657154-96657155	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs2251264	chr2:96657196-96657197	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs576358671	chr2:96657251-96657252	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs542264689	chr2:96657310-96657311	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs115480888	chr2:96657360-96657361	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs527820949	chr2:96657371-96657372	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs547552481	chr2:96657379-96657380	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs564749169	chr2:96657424-96657425	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs533343234	chr2:96657488-96657489	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs549923319	chr2:96657521-96657522	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs570020355	chr2:96657526-96657527	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs535721784	chr2:96657542-96657543	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs2579524	chr2:96657551-96657552	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs548200158	chr2:96657555-96657556	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs2579523	chr2:96657561-96657562	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs2579522	chr2:96657565-96657566	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs62155511	chr2:96657575-96657576	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs553575719	chr2:96657589-96657590	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs2579521	chr2:96657592-96657593	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs539645776	chr2:96657634-96657635	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs556365678	chr2:96657652-96657653	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs2260865	chr2:96657701-96657702	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs576420225	chr2:96657747-96657748	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs542130148	chr2:96657766-96657767	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs562141305	chr2:96657817-96657818	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs575626500	chr2:96657818-96657819	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs541555773	chr2:96657827-96657828	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs369930503	chr2:96657830-96657831	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs372329869	chr2:96657928-96657929	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs2258985	chr2:96657981-96657982	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Neuroblastoma	18574593	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Epilepsy	22083797	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96557400-96656800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr2:96577800-96656600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr2:96582800-96656400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:96586000-96657200	Weak transcription	Ovary	ovary
5	chr2:96587800-96656600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:96600600-96657200	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr2:96606400-96657200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr2:96607400-96657200	Weak transcription	Brain Hippocampus Middle	brain
9	chr2:96611000-96656600	Weak transcription	Osteobl	bone
10	chr2:96611400-96657200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr2:96616800-96657200	Weak transcription	Fetal Muscle Trunk	muscle
12	chr2:96617000-96656600	Weak transcription	Fetal Stomach	stomach
13	chr2:96617000-96656800	Weak transcription	Fetal Muscle Leg	muscle
14	chr2:96617200-96656800	Weak transcription	Brain Cingulate Gyrus	brain
15	chr2:96617800-96656600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:96621800-96657200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr2:96624000-96658200	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr2:96624400-96656600	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr2:96625200-96656600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr2:96626200-96656600	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr2:96628000-96657200	Weak transcription	Stomach Smooth Muscle	stomach
22	chr2:96628200-96656400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:96628200-96657200	Weak transcription	Left Ventricle	heart
24	chr2:96641600-96657200	Weak transcription	Fetal Heart	heart
25	chr2:96643000-96656400	Weak transcription	HMEC	breast
26	chr2:96644000-96656400	Weak transcription	Brain Germinal Matrix	brain
27	chr2:96644000-96656800	Weak transcription	Right Ventricle	heart
28	chr2:96644200-96656600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr2:96644800-96657200	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr2:96645400-96656600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:96645600-96656400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:96645600-96656800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr2:96645800-96656400	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr2:96645800-96657200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr2:96645800-96657200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr2:96646000-96656400	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr2:96646000-96656600	Weak transcription	Brain Anterior Caudate	brain
38	chr2:96646000-96657200	Weak transcription	Adipose Nuclei	Adipose
39	chr2:96646400-96656600	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr2:96646400-96656600	Weak transcription	Duodenum Mucosa	Duodenum
41	chr2:96646400-96656600	Weak transcription	A549	lung
42	chr2:96646400-96656600	Weak transcription	HSMM	muscle
43	chr2:96646400-96657200	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr2:96646600-96656400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr2:96646600-96656400	Weak transcription	NH-A	brain
46	chr2:96646600-96657200	Weak transcription	Primary T cells from cord blood	blood
47	chr2:96646600-96657200	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr2:96646600-96657200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr2:96646600-96657200	Weak transcription	Liver	Liver
50	chr2:96646800-96656800	Weak transcription	Primary T helper cells fromperipheralblood	blood

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