Variant report

Variant	nsv972432
Chromosome Location	chr9:99874607-99958095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:361)
CpG islands
(count:366)
Chromatin interactive
region (count:0)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:99898753-99898939	K562	blood:	n/a	n/a
2	BACH1	chr9:99955341-99955359	K562	blood:	n/a	n/a
3	BATF	chr9:99956088-99956460	GM12878	blood:	n/a	chr9:99956249-99956260 chr9:99956275-99956286
4	BATF	chr9:99928821-99929031	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:99930605-99930636	K562	blood:	n/a	n/a
6	BHLHE40	chr9:99893399-99893509	K562	blood:	n/a	n/a
7	BHLHE40	chr9:99938665-99938753	K562	blood:	n/a	n/a
8	BHLHE40	chr9:99890837-99890988	K562	blood:	n/a	n/a
9	CCNT2	chr9:99930594-99930784	K562	blood:	n/a	n/a
10	CEBPB	chr9:99941827-99942208	MCF-7	breast:	n/a	n/a
11	CEBPB	chr9:99941985-99942301	MCF-7	breast:	n/a	n/a
12	CEBPB	chr9:99941817-99942075	K562	blood:	n/a	n/a
13	CEBPB	chr9:99938608-99938672	K562	blood:	n/a	n/a
14	CEBPB	chr9:99883604-99883884	K562	blood:	n/a	n/a
15	CEBPB	chr9:99883701-99883784	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:99912920-99913060	HepG2	liver:	n/a	chr9:99912955-99912966
17	CEBPB	chr9:99883734-99883778	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:99883699-99883898	A549	lung:	n/a	n/a
19	CEBPD	chr9:99930459-99930728	K562	blood:	n/a	n/a
20	CEBPD	chr9:99930342-99930881	K562	blood:	n/a	n/a
21	CHD2	chr9:99905674-99905850	K562	blood:	n/a	n/a
22	CTCF	chr9:99915580-99915730	GM12874	blood:	n/a	chr9:99915654-99915663
23	CTCF	chr9:99915560-99915710	HepG2	liver:	n/a	chr9:99915654-99915663
24	CTCF	chr9:99916720-99916785	Lung_OC	lung:	n/a	n/a
25	CTCF	chr9:99915614-99915703	GM12891	blood:	n/a	chr9:99915654-99915663
26	CTCF	chr9:99915565-99915845	K562	blood:	n/a	chr9:99915654-99915663
27	CTCF	chr9:99915540-99915690	MCF-7	breast:	n/a	chr9:99915654-99915663
28	CTCF	chr9:99944701-99944775	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr9:99880195-99880228	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr9:99915500-99915650	GM12865	blood:	n/a	n/a
31	CTCF	chr9:99899684-99899741	GM20000	blood:	n/a	n/a
32	CTCF	chr9:99891832-99891865	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr9:99915600-99915718	MCF-7	breast:	n/a	chr9:99915654-99915663
34	CTCF	chr9:99938832-99938843	GM10248	blood:	n/a	n/a
35	CTCF	chr9:99915520-99915670	GM06990	blood:	n/a	chr9:99915654-99915663
36	CTCF	chr9:99915520-99915670	Hela-S3	cervix:	n/a	chr9:99915654-99915663
37	CTCF	chr9:99923540-99923588	GM13977	blood:	n/a	chr9:99923542-99923563 chr9:99923552-99923560 chr9:99923548-99923564
38	CTCF	chr9:99915579-99915704	GM19240	blood:	n/a	chr9:99915654-99915663
39	CTCF	chr9:99915601-99915714	GM10266	blood:	n/a	chr9:99915654-99915663
40	CTCF	chr9:99915573-99915746	MCF-7	breast:	n/a	chr9:99915654-99915663
41	CTCF	chr9:99923400-99923550	HMEC	breast:	n/a	n/a
42	CTCF	chr9:99915584-99915730	GM12878	blood:	n/a	chr9:99915654-99915663
43	CTCF	chr9:99915570-99915750	MCF-7	breast:	n/a	chr9:99915654-99915663
44	CTCF	chr9:99915620-99915770	GM12864	blood:	n/a	chr9:99915654-99915663
45	CTCF	chr9:99915546-99915821	K562	blood:	n/a	chr9:99915654-99915663
46	CTCF	chr9:99915562-99915736	HepG2	liver:	n/a	chr9:99915654-99915663
47	CTCF	chr9:99915620-99915770	K562	blood:	n/a	chr9:99915654-99915663
48	CTCF	chr9:99915540-99915690	RPTEC	kidney:	n/a	chr9:99915654-99915663
49	CTCF	chr9:99923541-99923586	Hela-S3	cervix:	n/a	chr9:99923542-99923563 chr9:99923552-99923560 chr9:99923548-99923564
50	CTCF	chr9:99915570-99915740	MCF-7	breast:	n/a	chr9:99915654-99915663

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:99915901-99915951	GM06990	blood:	n/a
2	chr9:99895750-99895800	A549	lung:	n/a
3	chr9:99883762-99883812	BE2_C	brain:	n/a
4	chr9:99895750-99895800	MCF-7	breast:	n/a
5	chr9:99883682-99883732	SK-N-SH	brain:	n/a
6	chr9:99915901-99915951	T-47D	breast:	n/a
7	chr9:99895750-99895800	ECC-1	luminal epithelium:	n/a
8	chr9:99884008-99884058	NT2-D1	testis:	n/a
9	chr9:99883762-99883812	HEEpiC	esophagus:	n/a
10	chr9:99883762-99883812	HIPEpiC	eye:	n/a
11	chr9:99884008-99884058	PFSK-1	brain:	n/a
12	chr9:99894337-99894387	SKMC	muscle:	n/a
13	chr9:99883762-99883812	GM12891	blood:	n/a
14	chr9:99895750-99895800	Hepatocyte	liver:	n/a
15	chr9:99884008-99884058	MCF-7	breast:	n/a
16	chr9:99894337-99894387	HEEpiC	esophagus:	n/a
17	chr9:99883682-99883732	HUVEC	blood vessel:	n/a
18	chr9:99883762-99883812	Hela-S3	cervix:	n/a
19	chr9:99884008-99884058	AG04449	skin:	fetal
20	chr9:99895750-99895800	GM12891	blood:	n/a
21	chr9:99915901-99915951	PrEC	prostate:	n/a
22	chr9:99884008-99884058	HRE	kidney:	n/a
23	chr9:99883682-99883732	RPTEC	kidney:	n/a
24	chr9:99884008-99884058	Hela-S3	cervix:	n/a
25	chr9:99884008-99884058	T-47D	breast:	n/a
26	chr9:99883762-99883812	NH-A	brain:	n/a
27	chr9:99894337-99894387	SAEC	small airway:	n/a
28	chr9:99884008-99884058	GM12891	blood:	n/a
29	chr9:99884008-99884058	HPAEpiC	pulmonary alveolar:	n/a
30	chr9:99915901-99915951	SK-N-SH_RA	brain:	n/a
31	chr9:99883762-99883812	K562	blood:	n/a
32	chr9:99915901-99915951	NB4	blood:	n/a
33	chr9:99883682-99883732	HRCEpiC	kidney:	n/a
34	chr9:99915901-99915951	U87	brain:	n/a
35	chr9:99894337-99894387	CMK	blood:	n/a
36	chr9:99883762-99883812	AG04449	skin:	fetal
37	chr9:99895750-99895800	HUVEC	blood vessel:	n/a
38	chr9:99895750-99895800	HEEpiC	esophagus:	n/a
39	chr9:99895750-99895800	HRCEpiC	kidney:	n/a
40	chr9:99884008-99884058	HIPEpiC	eye:	n/a
41	chr9:99894337-99894387	HRCEpiC	kidney:	n/a
42	chr9:99883682-99883732	HCPEpiC	choroid plexus:	n/a
43	chr9:99884008-99884058	HCPEpiC	choroid plexus:	n/a
44	chr9:99915901-99915951	BJ	skin:	n/a
45	chr9:99884008-99884058	HAEpiC	amniotic membrane:	n/a
46	chr9:99895750-99895800	CMK	blood:	n/a
47	chr9:99895750-99895800	HRE	kidney:	n/a
48	chr9:99915901-99915951	HL-60	blood:	n/a
49	chr9:99884008-99884058	SKMC	muscle:	n/a
50	chr9:99883762-99883812	HRE	kidney:	n/a

No data

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTSL2-4	chr9:99949736-99949789	ENSG00000159712.9
2	lnc-CTSL2-2	chr9:99891029-99892015	NONHSAT133470
3	lnc-CTSL2-4	chr9:99956985-99957122	ENSG00000159712.9
4	lnc-CTSL2-4	chr9:99940546-99940695	ENSG00000159712.9
5	lnc-CTSL2-5	chr9:99920066-99920111	NONHSAT133483
6	lnc-CTSL2-3	chr9:99957620-99958989	NONHSAT133488
7	lnc-CTSL2-5	chr9:99915509-99916020	NONHSAT133483
8	lnc-CTSL2-4	chr9:99954013-99954080	ENSG00000159712.9
9	lnc-CTSL2-4	chr9:99932889-99933018	ENSG00000159712.9
10	lnc-CTSL2-6	chr9:99906742-99907022	NONHSAT133477
11	lnc-CTSL2-5	chr9:99916172-99916337	NONHSAT133483
12	lnc-CTSL2-4	chr9:99924847-99925128	ENSG00000159712.9
13	lnc-CTSL2-4	chr9:99918175-99918867	ENSG00000159712.9
14	lnc-CTSL2-5	chr9:99924037-99924230	NONHSAT133483
15	lnc-CTSL2-5	chr9:99918814-99918867	NONHSAT133483
16	lnc-CTSL2-6	chr9:99906923-99907022	NONHSAT133476
17	lnc-CTSL2-6	chr9:99910243-99911530	NONHSAT133477
18	lnc-CTSL2-3	chr9:99957633-99957872	ENSG00000242375.1
19	lnc-CTSL2-6	chr9:99901930-99902236	NONHSAT133476
20	lnc-CTSL2-4	chr9:99947724-99947797	ENSG00000159712.9
21	lnc-CTSL2-2	chr9:99890338-99890362	NONHSAT133470
22	lnc-CTSL2-4	chr9:99922464-99922684	ENSG00000159712.9
23	lnc-C9orf174-3	chr9:99883941-99884771	NONHSAT133468
24	lnc-CTSL2-4	chr9:99924037-99924248	ENSG00000159712.9
25	lnc-CTSL2-5	chr9:99917886-99918005	NONHSAT133483
26	lnc-CTSL2-2	chr9:99885291-99885366	NONHSAT133463
27	lnc-CTSL2-6	chr9:99906140-99906208	NONHSAT133476
28	lnc-CTSL2-4	chr9:99942283-99943198	ENSG00000159712.9
29	lnc-CTSL2-4	chr9:99935228-99935342	ENSG00000159712.9
30	lnc-CTSL2-6	chr9:99910243-99911530	NONHSAT133476
31	lnc-CTSL2-5	chr9:99922464-99922684	NONHSAT133483

No data

Variant related genes	Relation type
RNU6-798P	TF binding region
FAM220CP	TF binding region
RNU6-798P	CpG island
FAM220CP	CpG island

Extended variants
information (count: 2919 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2919 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370919737	chr9:99874641-99874642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551561958	chr9:99874652-99874653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529113277	chr9:99874658-99874659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115940127	chr9:99874680-99874681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569799096	chr9:99874681-99874682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201599909	chr9:99874694-99874695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532927148	chr9:99874715-99874716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551341955	chr9:99874735-99874736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537230883	chr9:99874770-99874771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566374434	chr9:99874811-99874812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549245205	chr9:99874815-99874816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372465011	chr9:99874841-99874842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534957815	chr9:99874875-99874876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73654651	chr9:99874890-99874891	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs568268009	chr9:99874983-99874984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535041976	chr9:99874998-99874999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs117123174	chr9:99875034-99875035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183364779	chr9:99875042-99875043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575676726	chr9:99875056-99875057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73654652	chr9:99875097-99875098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571981595	chr9:99875126-99875127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141371134	chr9:99875173-99875174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539006416	chr9:99875237-99875238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187910353	chr9:99875251-99875252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573287761	chr9:99875252-99875253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191269157	chr9:99875272-99875273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561968368	chr9:99875273-99875274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184411252	chr9:99875347-99875348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544412842	chr9:99875356-99875357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113173532	chr9:99875357-99875358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139311526	chr9:99875399-99875400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551210439	chr9:99875469-99875470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142443126	chr9:99875480-99875481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189735945	chr9:99875481-99875482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554086476	chr9:99875530-99875531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192656211	chr9:99875611-99875612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566250841	chr9:99875695-99875696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185045850	chr9:99875779-99875780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551130303	chr9:99875810-99875811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536512600	chr9:99875822-99875823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371265369	chr9:99875848-99875849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201795219	chr9:99875856-99875857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535323752	chr9:99875857-99875858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138075851	chr9:99875938-99875939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78890538	chr9:99875944-99875945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539884420	chr9:99875985-99875986	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6477931	chr9:99876022-99876023	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs566828184	chr9:99876051-99876052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112829959	chr9:99876084-99876085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10759476	chr9:99876128-99876129	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Neurodevelopmental disorder	22521361	CNVD
Nicotine dependence	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99850600-99877000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:99867800-99887600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr9:99871600-99876400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr9:99871600-99877800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr9:99871800-99879800	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr9:99872000-99875800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr9:99872000-99876400	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr9:99872000-99876800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr9:99872000-99879800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr9:99872000-99890200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr9:99874800-99875000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr9:99875000-99876400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:99875000-99880200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr9:99875800-99895800	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr9:99876400-99878200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr9:99876400-99880600	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr9:99876400-99885600	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr9:99876800-99888200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr9:99877000-99877400	Strong transcription	H9 Cell Line	embryonic stem cell
20	chr9:99877400-99878400	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr9:99877800-99878200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
22	chr9:99878200-99879800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:99878200-99880000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr9:99878400-99878800	Strong transcription	H9 Cell Line	embryonic stem cell
25	chr9:99878800-99880000	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr9:99879800-99880600	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr9:99879800-99880800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
28	chr9:99879800-99880800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr9:99880000-99880600	Strong transcription	H9 Cell Line	embryonic stem cell
30	chr9:99880000-99881000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr9:99880200-99880400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr9:99880400-99890600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr9:99880600-99882000	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr9:99880600-99883400	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr9:99880600-99883800	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr9:99880800-99882800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr9:99880800-99882800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr9:99881000-99884600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr9:99881200-99883400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr9:99882000-99885200	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr9:99882000-99896600	Weak transcription	Right Atrium	heart
42	chr9:99882000-99897400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr9:99882800-99884600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
44	chr9:99882800-99885200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr9:99883200-99886000	Weak transcription	Brain Anterior Caudate	brain
46	chr9:99883400-99883800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr9:99883400-99884600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr9:99883400-99885200	Strong transcription	H1 Cell Line	embryonic stem cell
49	chr9:99883800-99884000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:99883800-99884000	ZNF genes & repeats	Dnd41	blood

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