Variant report

Variant	esv3447668
Chromosome Location	chrX:138284786-138286884
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:141)
CpG islands
(count:549)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:141 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chrX:138285444-138285520	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chrX:138285845-138286260	K562	blood:	n/a	n/a
3	CBX3	chrX:138285971-138286300	K562	blood:	n/a	n/a
4	CCNT2	chrX:138286505-138286778	K562	blood:	n/a	n/a
5	CCNT2	chrX:138285810-138286281	K562	blood:	n/a	n/a
6	CTBP2	chrX:138284616-138286747	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chrX:138285240-138285390	AG09319	gingival:	n/a	n/a
8	CTCF	chrX:138285940-138286090	HMEC	breast:	n/a	n/a
9	CTCF	chrX:138285900-138286050	AoAF	blood vessel:	n/a	n/a
10	CTCF	chrX:138286040-138286190	HRE	kidney:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
11	CTCF	chrX:138285231-138285649	H1-hESC	embryonic stem cell:	n/a	chrX:138285442-138285455 chrX:138285444-138285457
12	CTCF	chrX:138285912-138286237	K562	blood:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
13	CTCF	chrX:138285940-138286090	HRPEpiC	eye:	n/a	n/a
14	CTCF	chrX:138284767-138284872	LNCaP	prostate:	n/a	n/a
15	CTCF	chrX:138286034-138286050	MCF-7	breast:	n/a	n/a
16	CTCF	chrX:138285868-138286204	H1-hESC	embryonic stem cell:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
17	CTCF	chrX:138285906-138286233	MCF-7	breast:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
18	CTCF	chrX:138285812-138286196	Fibrobl	skin:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
19	CTCF	chrX:138286160-138286310	AG10803	skin:	n/a	n/a
20	CTCF	chrX:138286130-138286204	GM12891	blood:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
21	CTCF	chrX:138285887-138285889	MCF-7	breast:	n/a	n/a
22	CTCF	chrX:138285940-138286090	K562	blood:	n/a	n/a
23	CTCF	chrX:138286100-138286250	MCF-7	breast:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
24	CTCF	chrX:138285900-138286050	K562	blood:	n/a	n/a
25	CTCF	chrX:138285920-138286070	HEK293	kidney:	n/a	n/a
26	CTCF	chrX:138285980-138286130	SAEC	small airway:	n/a	n/a
27	CTCF	chrX:138285536-138285546	MCF-7	breast:	n/a	n/a
28	CTCF	chrX:138285960-138286110	GM12864	blood:	n/a	n/a
29	CTCF	chrX:138285824-138286263	MCF-7	breast:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
30	CTCF	chrX:138286080-138286230	HEEpiC	esophagus:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
31	CTCF	chrX:138286140-138286290	NHEK	skin:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
32	CTCF	chrX:138285940-138286090	HMF	breast:	n/a	n/a
33	CTCF	chrX:138285554-138285558	MCF-7	breast:	n/a	n/a
34	CTCF	chrX:138285828-138286253	MCF-7	breast:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
35	CTCF	chrX:138285906-138286021	NHEK	skin:	n/a	n/a
36	CTCF	chrX:138286111-138286124	ProgFib	skin:	n/a	n/a
37	CTCF	chrX:138285940-138286090	HCM	heart:	n/a	n/a
38	CTCF	chrX:138285860-138286010	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chrX:138285298-138285390	Fibrobl	skin:	n/a	n/a
40	CTCF	chrX:138285870-138286120	A549	lung:	n/a	n/a
41	CTCF	chrX:138285880-138286030	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chrX:138285260-138285410	HAc	cerebellar:	n/a	n/a
43	CTCF	chrX:138285880-138286030	GM12865	blood:	n/a	n/a
44	CTCF	chrX:138286160-138286310	K562	blood:	n/a	n/a
45	CTCF	chrX:138286060-138286210	Caco-2	colon:	n/a	chrX:138286141-138286154 chrX:138286141-138286154
46	CTCF	chrX:138285840-138285990	HAc	cerebellar:	n/a	n/a
47	CTCF	chrX:138285837-138286107	ProgFib	skin:	n/a	n/a
48	CTCF	chrX:138285880-138286030	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chrX:138285941-138286044	Medullo	brain:	n/a	n/a
50	CTCF	chrX:138285900-138286050	AG09319	gingival:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:138285828-138285878	BJ	skin:	n/a
2	chrX:138285233-138285283	HEEpiC	esophagus:	n/a
3	chrX:138285828-138285878	K562	blood:	n/a
4	chrX:138285540-138285590	SKMC	muscle:	n/a
5	chrX:138285233-138285283	AG09319	gingival:	n/a
6	chrX:138285861-138285911	IMR90	lung:	fetal
7	chrX:138286295-138286345	NH-A	brain:	n/a
8	chrX:138285233-138285283	CMK	blood:	n/a
9	chrX:138285393-138285443	AG09319	gingival:	n/a
10	chrX:138285393-138285443	BJ	skin:	n/a
11	chrX:138286295-138286345	RPTEC	kidney:	n/a
12	chrX:138285540-138285590	HL-60	blood:	n/a
13	chrX:138286295-138286345	AG04449	skin:	fetal
14	chrX:138285393-138285443	HEEpiC	esophagus:	n/a
15	chrX:138286295-138286345	CMK	blood:	n/a
16	chrX:138285469-138285519	K562	blood:	n/a
17	chrX:138285393-138285443	GM19239	blood:	n/a
18	chrX:138285233-138285283	HRE	kidney:	n/a
19	chrX:138285828-138285878	PrEC	prostate:	n/a
20	chrX:138285540-138285590	PFSK-1	brain:	n/a
21	chrX:138285861-138285911	H1-hESC	embryonic stem cell:	embryo
22	chrX:138285469-138285519	ECC-1	luminal epithelium:	n/a
23	chrX:138286295-138286345	HNPCEpiC	eye:	n/a
24	chrX:138285922-138285972	Hepatocyte	liver:	n/a
25	chrX:138285393-138285443	RPTEC	kidney:	n/a
26	chrX:138285469-138285519	NB4	blood:	n/a
27	chrX:138285393-138285443	Hepatocyte	liver:	n/a
28	chrX:138286760-138286810	HEEpiC	esophagus:	n/a
29	chrX:138285828-138285878	HRPEpiC	eye:	n/a
30	chrX:138285922-138285972	SK-N-SH	brain:	n/a
31	chrX:138286295-138286345	GM06990	blood:	n/a
32	chrX:138286760-138286810	IMR90	lung:	fetal
33	chrX:138285828-138285878	SK-N-SH_RA	brain:	n/a
34	chrX:138285861-138285911	SK-N-SH_RA	brain:	n/a
35	chrX:138285469-138285519	U87	brain:	n/a
36	chrX:138286760-138286810	HepG2	liver:	n/a
37	chrX:138285233-138285283	MCF10A-Er-Src	breast:	n/a
38	chrX:138285828-138285878	ovcar-3	ovarian:	n/a
39	chrX:138285828-138285878	LNCaP	prostate:	n/a
40	chrX:138285828-138285878	HCT-116	colon:	n/a
41	chrX:138285393-138285443	NHDF-neo	bronchial:	n/a
42	chrX:138285861-138285911	RPTEC	kidney:	n/a
43	chrX:138285922-138285972	CMK	blood:	n/a
44	chrX:138285922-138285972	HCT-116	colon:	n/a
45	chrX:138285393-138285443	HRCEpiC	kidney:	n/a
46	chrX:138286760-138286810	HNPCEpiC	eye:	n/a
47	chrX:138285469-138285519	NHDF-neo	bronchial:	n/a
48	chrX:138286760-138286810	SK-N-SH	brain:	n/a
49	chrX:138285393-138285443	SKMC	muscle:	n/a
50	chrX:138285828-138285878	SKMC	muscle:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:138273663..138275580-chrX:138283129..138285298,2	K562	blood:
2	chr16:57126223..57126746-chrX:138285972..138286492,2	Hela-S3	cervix:
3	chrX:138285411..138288031-chrX:138303226..138305707,3	K562	blood:
4	chrX:138282011..138285172-chrX:138285245..138287356,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCF2-3	chrX:138286222-138286433	NONHSAT138775

No data

Variant related genes	Relation type
FGF13	TF binding region
FGF13	CpG island
ENSG00000129682	chromatin interactions
ENSG00000140848	chromatin interactions

Extended variants
information (count: 28 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111407611	chrX:138284870-138284871	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs185612343	chrX:138284989-138284990	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189588936	chrX:138285033-138285034	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs372289476	chrX:138285040-138285041	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs148812436	chrX:138285051-138285052	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1894467	chrX:138285103-138285104	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs201017911	chrX:138285110-138285111	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs199812228	chrX:138285112-138285113	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs5976307	chrX:138285272-138285273	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184418628	chrX:138285287-138285288	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201335069	chrX:138285291-138285292	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189077988	chrX:138285298-138285299	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181118739	chrX:138285343-138285344	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186510395	chrX:138285393-138285394	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72616268	chrX:138285441-138285442	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs73574154	chrX:138285495-138285496	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181017131	chrX:138285675-138285676	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538841047	chrX:138285699-138285700	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs367636726	chrX:138285700-138285701	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs12395539	chrX:138285936-138285937	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs73634018	chrX:138286026-138286027	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs372671282	chrX:138286157-138286158	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs386827908	chrX:138286198-138286199	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs114849724	chrX:138286199-138286200	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs374963111	chrX:138286207-138286208	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs367969838	chrX:138286279-138286280	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs41304506	chrX:138286348-138286349	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs373259552	chrX:138286548-138286549	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Cancer	16751803	CNVD
small cell lung cancer	20016488	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	17603634	CNVD
abnormal development	18461090	CNVD
Multiple myeloma	17550852	CNVD
Premature ovarian failure	20952765	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Hereditary coagulopathy	21993689	CNVD
Cerebellar atrophy	21569638	CNVD
Fragile x	21569638	CNVD
Abnormal corpus callosum	21572526	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:138277400-138285200	Weak transcription	Pancreas	Pancrea
2	chrX:138277600-138285400	Weak transcription	Liver	Liver
3	chrX:138277600-138286000	Weak transcription	Right Atrium	heart
4	chrX:138279000-138284800	Weak transcription	Gastric	stomach
5	chrX:138282600-138284800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chrX:138282600-138284800	Weak transcription	Psoas Muscle	Psoas
7	chrX:138282800-138285000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chrX:138282800-138285400	Weak transcription	Esophagus	oesophagus
9	chrX:138283000-138285000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chrX:138283000-138288600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chrX:138284200-138285000	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chrX:138284400-138284800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
13	chrX:138284400-138284800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
14	chrX:138284400-138284800	Flanking Active TSS	K562	blood
15	chrX:138284400-138285000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
16	chrX:138284400-138285000	Enhancers	HSMMtube	muscle
17	chrX:138284400-138285200	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chrX:138284400-138285400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chrX:138284400-138287800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chrX:138284400-138288400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
21	chrX:138284600-138284800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chrX:138284600-138284800	Bivalent/Poised TSS	Adipose Nuclei	Adipose
23	chrX:138284600-138284800	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
24	chrX:138284600-138285000	Bivalent Enhancer	NH-A	brain
25	chrX:138284600-138285200	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chrX:138284600-138285200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
27	chrX:138284600-138285200	Flanking Active TSS	Brain Germinal Matrix	brain
28	chrX:138284600-138286400	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chrX:138284600-138287800	Bivalent/Poised TSS	Fetal Brain Female	brain
30	chrX:138284600-138288000	Bivalent/Poised TSS	Fetal Intestine Large	intestine
31	chrX:138284600-138288200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
32	chrX:138284600-138288600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
33	chrX:138284600-138288800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
34	chrX:138284600-138288800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
35	chrX:138284800-138285000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
36	chrX:138284800-138285000	Bivalent Enhancer	Fetal Brain Male	brain
37	chrX:138284800-138285000	Bivalent/Poised TSS	Fetal Stomach	stomach
38	chrX:138284800-138285000	Enhancers	Gastric	stomach
39	chrX:138284800-138285200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chrX:138284800-138285200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chrX:138284800-138285200	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chrX:138284800-138285400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
43	chrX:138284800-138286000	Bivalent/Poised TSS	Placenta	Placenta
44	chrX:138284800-138287800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chrX:138284800-138287800	Active TSS	K562	blood
46	chrX:138284800-138288000	Active TSS	Psoas Muscle	Psoas
47	chrX:138284800-138288400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
48	chrX:138284800-138288600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
49	chrX:138285000-138285200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
50	chrX:138285000-138285200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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